Offers “Roche”

Expires soon Roche

Project Management Manager

  • Beijing, 中华人民共和国
  • Marketing

Job description

  Job facts

Job Summary :

Provides leadership to one or more clinical trial projects and provides strategic planning and organization to achieve successful study completion. Has full ownership of the accountability projects and ensures the effective and efficient delivery of all operational aspects in accordance with ICH/GCP standards, Roche SOPs, and local regulatory requirements. Also ensures the development and maintenance of productive good relationships with internal or external customers.

Main Tasks & Responsibilities :

Builds effective, high performing study team through influence, integration, motivation and optimization of team performance. Embeds the Roche values into the team(s) culture and promotes the team spirit.
Set up the project management and co-monitoring plan, and follow up the execution to control project quality and timeline.
Develops and manages study budget plan, and forecasts using appropriate tools, ensures the study has the appropriate resources to effectively deliver high quality studies on time and within budget.
Develops study timelines and ensures that milestones are set and managed properly and delivered on time.
Lead site selection and develops/maintains investigator relations, builds and maintains a professional relationship between Roche and Investigator.
Lead/coordinate study team to develop study protocol, report or other study tools.
Be responsible study supply management, including internal or external supplies order and distribution.
The logistical management of study instruments, including order, installation and recycle. Closely cooperation with CC.
Be responsible for data management or statistical management CRO selection and agreement negotiation.

Basic Requirements of the Job :

Education& Qualifications

University degree or equivalent in a medical/science-related field and or 5 years proven experience in Clinical Research/Development or related industry.
Proficiency in both spoken and written English
3. Good command of MS office software application
Understand medical device regulation

Experience

At least 5 years of working experience in either Medical Device or Diagnostics industry, and 2 years of working experience in clinical study of IVD/Medical Device/Drug.

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